An immunochromatographic test paper for detecting pyrethroids
An immunochromatographic test paper and pyrethroid technology, which is applied in the directions of measuring devices, analytical materials, instruments, etc., can solve the problem of high technical requirements for pretreatment and operators, poor repeatability and reproducibility of analytical results, and expensive instruments and equipment, etc. problems, to achieve the effect of protecting the health of consumers, obvious economic and social benefits, and showing the image of the results
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Embodiment 1
[0045] The immunochromatographic test paper for detecting pyrethroids of the present invention, with reference to Figure 1-2 , including a support and an adsorption layer fixed on the support, the adsorption layer is a sample pad 1, a binding pad 2, a chromatographic membrane 3 and an absorption pad 4 in order from the test end, and it is characterized in that the binding pad is adsorbed with Nanomaterial-labeled anti-PBA monoclonal antibody PBA-mAb; the chromatographic membrane is provided with a stealth detection blot 5 printed with a carrier protein (PBA artificial antigen) solution coupled to PBA and a goat anti- or rabbit anti-mouse Stealth control blot 6 printed by IgG antibody solution; the nanomaterials are nitrogen-doped carbon nanomaterials, carbon nanomaterials, and carbon quantum dot fluorescent nanoparticles.
[0046] The support body includes a bottom layer 7 arranged on the bottom surface of the adsorption layer and a surface layer 8 arranged on the top surface...
Embodiment 2
[0057] This embodiment detects pyrethroid test paper, mainly including: the preparation of PBA artificial antigen, PBA monoclonal antibody (PBA-mAb), the preparation of nitrogen-doped carbon nanomaterials (N-CDs) labeled PBA antibody and based on N-CDs labeling The steps such as the preparation of immunochromatographic test paper, wherein, the preparation method of each product is as follows:
[0058] 1. Preparation of PBA artificial antigen (PBA-BSA)
[0059] 10 mg of bovine serum albumin (BSA) was weighed and placed in a 10 mL screw bottle, and pH 9.0 carbonate buffer solution was used to prepare 10% BSA activation solution A with a mass fraction. Weigh 1mg of fenpropathrin (PBA) and add 2mL of 0.1mol / L NaIO 4 Dissolve to make Solution B. Add solution A to solution B and let it react at room temperature for 30min, then add 0.1mL NaBH 4 The buffer was stirred and mixed, adjusted to pH 9.0 with 1mol / L NaOH, reacted at 4°C overnight, dialyzed with 0.01mol / L pH 7.4 phosphate ...
Embodiment 3
[0084] The detection of pyrethroid test paper in this embodiment mainly includes: preparation of PBA artificial antigen, PBA monoclonal antibody (PBA-mAb), preparation of carbon nanomaterial-labeled PBA antibody, and preparation of immunochromatographic test paper based on carbon nanomaterial labeling, etc. Step, wherein, the preparation method of each product is as follows:
[0085] 1. Preparation of PBA artificial antigen (PBA-BSA)
[0086] With embodiment 2.
[0087] 2. Preparation of PBA-mAb
[0088] With embodiment 2.
[0089] 3. Preparation of immunochromatographic test paper based on carbon nanomaterial labeling
[0090] (1) Preparation of carbon nanomaterial TPCA
[0091] Dissolve 1.5g citric acid and 1.62g cysteamine hydrochloride in 7.5mL ultrapure water, transfer the solution to a 50mL polytetrafluoroethylene liner after fully dissolving, and then place the liner in a high-pressure reactor. React at 200°C for 3 hours. After the reaction, the product was suction...
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